SCHEMBL379626

SCHEMBL379626

O=C1CCCOc2ccccc21

nearest known ligand 0.48

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAOB P27338 6/20 0.48
MAOA P21397 2/20 0.48
PKM P14618 1/20 0.48
TSHR P16473 1/20 0.48
CYP2A6 P11509 1/20 0.48
GRM5 P41594 4/20 0.45
ITGB2 P05107 1/20 0.44
ICAM1 P05362 1/20 0.44
ITGAL P20701 1/20 0.44
NPC1 O15118 2/20 0.42
RAB9A P51151 2/20 0.42
SMN1; SMN2 Q16637 3/20 0.41
ALDH1A1 P00352 1/20 0.41
HPGD P15428 1/20 0.41
NFKB1 P19838 1/20 0.41
NFKB2 Q00653 1/20 0.41
RELA Q04206 1/20 0.41
NPSR1 Q6W5P4 1/20 0.41
CYP19A1 P11511 2/20 0.41
KDM4E B2RXH2 1/20 0.41

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
Chromanone SCHEMBL28794 0.88 MAOB (0.56) MAOBMAOAPKMTSHRCYP2A6
Chromanone SCHEMBL28205525 0.88 MAOB (0.56) MAOBMAOAPKMTSHRCYP2A6
Chromanone SCHEMBL29384996 0.88 MAOB (0.56) MAOBMAOAPKMTSHRCYP2A6
Chromanone SCHEMBL28719460 0.86 MAOB (0.55) MAOBMAOAPKMTSHRCYP2A6
Chromanone SCHEMBL27846233 0.86 MAOB (0.55) MAOBMAOAPKMTSHRCYP2A6
Chromanone SCHEMBL28463260 0.86 MAOB (0.55) MAOBMAOAPKMTSHRCYP2A6
Chromanone SCHEMBL30017864 0.86 MAOB (0.55) MAOBMAOAPKMTSHRCYP2A6
Chromanone SCHEMBL7617916 0.86 MAOB (0.55) MAOBMAOAPKMTSHRCYP2A6
Chromanone SCHEMBL29349977 0.86 MAOB (0.55) MAOBMAOAPKMTSHRCYP2A6
Chromanone SCHEMBL28145031 0.84 MAOB (0.53) MAOBMAOAPKMTSHRGRM5

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 155 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111518117-B 1, 2-oxazinopyran compound and preparation method and application thereof 西安凯新生物科技有限公司 2022-08-26 CN claimed
CN-111518117-A 1, 2-oxazinopyran compound and preparation method and application thereof 朱翠萍 2020-08-11 CN claimed
US-20050282863-A1 Novel-N substituted dihydrobenzothiepino, dihydrobenzoxepino and tetrahydro benzocyclohepta indoles as selective estrogen receptor modulators COUNCIL OF SCIENTIFIC & INDUSTRIAL RESEARCH (IN) 2005-12-22 US claimed
WO-2005094833-A1 NOVEL N-SUBSTITUTED DIHYDROBENZOTHIEPINO, DIHYDROBENZOXEPINO AND TETRAHYDRO BENZOCYCLOHEPTA INDOLES AS SELECTIVE ESTROGEN RECEPTOR MODULATORS COUNCIL OF SCIENTIFIC AND INDUSTRIAL RESEARCH (IN) 2005-10-13 WO claimed
WO-2001000775-A1 BENZOLACTONES AS BLEACH ACTIVATORS U.S. BORAX INC. (US) 2001-01-04 WO claimed
EP-0024560-B1 3-AMINO-1-BENZOXEPINE DERIVATIVES AND THEIR SALTS, PROCESSES FOR THEIR PREPARATION AND MEDICAMENTS CONTAINING THEM Kali-Chemie Pharma GmbH (DE) 1983-04-13 EP claimed
US-4279904-A GASTROINTESTINAL DISORDERS KALI-CHEMIE PHARMA GMBH (DE) 1981-07-21 US claimed
EP-0024560-A1 3-Amino-1-benzoxepine derivatives and their salts, processes for their preparation and medicaments containing them Kali-Chemie Pharma GmbH (DE) 1981-03-11 EP claimed
US-20260085073-A1 PYRAZOLYLCARBOXAMIDE COMPOUNDS AND THEIR USE IN THERAPY HOTSPOT THERAPEUTICS INC (US) 2026-03-26 US disclosed
US-12565488-B2 Inhibitors of influenza virus replication COCRYSTAL PHARMA, INC. (US) 2026-03-03 US disclosed
US-11725001-B2 Bicyclic compound and use thereof SK BIOPHARMACEUTICALS CO., LTD. (KR) 2023-08-15 US disclosed
WO-2023026884-A1 CURABLE COMPOSITION, METHOD FOR PRODUCING CURED PRODUCT, FILM, OPTICAL ELEMENT, IMAGE SENSOR, SOLID STATE IMAGE SENSOR, IMAGE DISPLAY DEVICE, AND RADICAL POLYMERIZATION INITIATOR 富士フイルム株式会社 2023-03-02 WO disclosed
WO-2022204150-A1 COMPOUNDS AND COMPOSITIONS FOR TREATING CNS DISORDERS BLUE OAK PHARMACEUTICALS, INC. (US) 2022-09-29 WO disclosed
CN-111518117-B 1, 2-oxazinopyran compound and preparation method and application thereof 西安凯新生物科技有限公司 2022-08-26 CN disclosed
US-4766212-A ANALGESICS, MUSCLE RELAXANTS, HYPOTENSIVE AGENTS MERRELL DOW PHARMACEUTICALS INC. (US) 1988-08-23 US disclosed
EP-0116373-B1 2H-(1) BENZOXEPINO(5,4-B)-1,4-OXAZINE DERIVATIVES MERRELL DOW PHARMACEUTICALS INC. (US) 1987-04-15 EP disclosed
EP-0116372-B1 2H-(1) BENZOXEPINO (5,4-B)-1,4 OXAZINE DERIVATIVES MERRELL DOW PHARMACEUTICALS INC. (US) 1987-01-21 EP disclosed
EP-0116372-A1 2H-(1) benzoxepino (5,4-b)-1,4 oxazine derivatives MERRELL DOW PHARMACEUTICALS INC. (US) 1984-08-22 EP disclosed
EP-0116373-A1 2H-(1) benzoxepino(5,4-b)-1,4-oxazine derivatives MERRELL DOW PHARMACEUTICALS INC. (US) 1984-08-22 EP disclosed
US-4179516-A Ethers of 3,4-dihydro-1-benzoxepin-5-one oxime to treat intestinal disorders ALBERT ROLLAND, S.A. (FR) 1979-12-18 US disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (4 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20050282863-A1 Novel-N substituted dihydrobenzothiepino, dihydrobenzoxepino and tetrahydro benzocyclohepta indoles as selective estrogen receptor modulators ESR1, ESR2, HSD17B11 MAOB 256/4885MAOA 369/4885PKM 3826/4885
US-12565488-B2 Inhibitors of influenza virus replication IFNAR1, HCFC1, NR3C1 MAOB 1299/4885MAOA 1335/4885PKM 4832/4885
US-11725001-B2 Bicyclic compound and use thereof PRMT5, PRMT6, PRMT1 MAOB 3338/4885MAOA 3468/4885PKM 777/4885
US-20260085073-A1 PYRAZOLYLCARBOXAMIDE COMPOUNDS AND THEIR USE IN THERAPY MALT1, BCL6, BCL3 MAOB 4757/4885MAOA 4734/4885PKM 3785/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.